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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561462생성일: 2026년 10월 26일

Water → 4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/561462

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물P-ChloroacetophenoneHCID 7467—
반응물HCID 178418630HCID 178418630—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanolHCID 23463—

반응 조건

온도0 °C

반응 단계

1.50 g (9.70 mmol) of 4-chloroacetophenone were dissolved in 8 ml of diethyl ether at 0° C., and 38.8 ml (19.41 mmol) of a 0.5N solution of cyclopropylmagnesium bromide in tetrahydrofuran were slowly added dropwise. Stirring at 0° C. for 1 h was followed by warming to RT, addition of water and acetonitrile to the reaction solution, and filtration of the mixture through kieselguhr. The organic solvents were removed in a rotary evaporator, and the aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed with saturated aqueous sodium chloride solution, and the solvents were removed in vacuo. The crude product was purified twice by preparative HPLC (mobile phase: acetonitrile/water gradient). The acetonitrile was removed from the combined product phases in a rotary evaporator, and the aqueous phase was extracted twice with diethyl ether. The combined organic phases were again washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and filtered, and the solvents were removed in vacuo. 1.37 g (72% of theory) of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063234B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-c7474b85547b455f9308765e46716d1f
출처 메모uspto-grants-2011_11